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What kind of a future for young people with Down's Syndrome? The views and aspirations of young people and families

Jill Davies (Foundation for People with Learning Disabilities, UK)
Hazel Morgan (Foundation for People with Learning Disabilities, UK)

Tizard Learning Disability Review

ISSN: 1359-5474

Article publication date: 9 November 2010

459

Abstract

This article describes a project that explored the views, experiences and aspirations of young people with Down's Syndrome and their family carers. Each young person had gone or was going through the transition to adulthood. Following a scoping study, young people who were leading the lives of their choice, for example through use of person‐centred planning or direct payments, were interviewed, and their stories were published in a booklet. The next phase brought other young people and their families together in workshops to support them in planning for their future, based on the information from the booklet. Interviews with the young people and their families dispelled the myth that parents are obstacles to progress and change. All families actively supported their son or daughter to achieve their aspirations and had high expectations for them.

Keywords

Citation

Davies, J. and Morgan, H. (2010), "What kind of a future for young people with Down's Syndrome? The views and aspirations of young people and families", Tizard Learning Disability Review, Vol. 15 No. 4, pp. 22-29. https://doi.org/10.5042/tldr.2010.0590

Publisher

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Emerald Group Publishing Limited

Copyright © 2010, Emerald Group Publishing Limited

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